期刊
ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 55, 期 9, 页码 6171-6183出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c00515
关键词
-
资金
- Natural Science Foundation of Heilongjiang Province of China [ZD2020C005]
The study focused on the toxic effects of Cypermethrin on grass carp, showing hepatotoxicity in terms of pathological changes, oxidative stress, and apoptosis in the liver. RNA-Seq analysis suggested that proteasome and oxidative phosphorylation pathways were compromised under CMN exposure, leading to toxic effects. In vitro studies further confirmed that proteasome pathway inhibition could protect against CMN-induced toxicity by enhancing antioxidative and anti-inflammatory capability.
Cypermethrin (CMN) is a man-made insecticide, and its abuse has led to potential adverse effects, particularly in sensitive populations such as aquatic organisms. The present study was focused on the toxic phenotype and detoxification mechanism in grass carp (Ctenopharyngodon idella) after treatment with waterborne CMN (0.651 mu g/L) for 6 weeks in vivo or 6.392 mu M for 24 h in vitro. In vivo, we describe the toxic phenotype of the liver of grass carp in terms of pathological changes, serum transaminase levels, oxidative stress indexes, and apoptosis rates. RNA-Seq analysis (2 x 3 cDNA libraries) suggested a compromise of proteasome and oxidative phosphorylation signaling pathways under CMN exposure. Thus, these two pathways were chosen for the in vitro study, which suggested that the CMN intoxication-induced proteasome pathway caused hepatotoxicity in the liver cell line of grass carp (L8824 cells). Moreover, pretreatment with MG132, a proteasome inhibitor, displayed protection against the toxic effects of CMN by enhancing antioxidative and anti-inflammatory capability by directly inhibiting the proteasomal degradation of nuclear factor erythroid-2 related factor (Nrf2) and I kappa B-alpha, thus turning on the transcription of downstream genes of Nrf2 and NF-kappa B, respectively. Taken together, these results suggest proteasome activity as a reason for CMN-induced hepatotoxicity.
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